Structure of PDB 2hlp Chain A Binding Site BS01
Receptor Information
>2hlp Chain A (length=303) Species:
2238
(Haloarcula marismortui) [
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TKVSVVGAAGTVGAAAGYNIALRDIADEVVFVDIPDKEDDTVGQAADTNH
GIAYDSNTRVRQGGYEDTAGSDVVVITAGIPRQPGQTRIDLAGDNAPIME
DIQSSLDEHNDDYISLTTSNPVDLLNRHLYEAGDRSREQVIGFGGRLDSA
RFRYVLSEEFDAPVQNVEGTILGEHGDAQVPVFSKVRVDGTDPEFSGDEK
EQLLGDLQESAMDVIERKGATEWGPARGVAHMVEAILHDTGRVLPASVKL
EGEFGHEDTAFGVPVRLGSNGVEEIVEWDLDDYEQDLMADAAEKLSDQYD
KIS
Ligand information
Ligand ID
CL
InChI
InChI=1S/ClH/h1H/p-1
InChIKey
VEXZGXHMUGYJMC-UHFFFAOYSA-M
SMILES
Software
SMILES
ACDLabs 10.04
CACTVS 3.341
OpenEye OEToolkits 1.5.0
[Cl-]
Formula
Cl
Name
CHLORIDE ION
ChEMBL
DrugBank
DB14547
ZINC
PDB chain
2hlp Chain A Residue 1002 [
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Receptor-Ligand Complex Structure
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PDB
2hlp
Halophilic adaptation: novel solvent protein interactions observed in the 2.9 and 2.6 A resolution structures of the wild type and a mutant of malate dehydrogenase from Haloarcula marismortui.
Resolution
2.59 Å
Binding residue
(original residue number in PDB)
K205 D306
Binding residue
(residue number reindexed from 1)
K185 D279
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
R109 D168 R171 H195
Catalytic site (residue number reindexed from 1)
R88 D148 R151 H175
Enzyme Commision number
1.1.1.37
: malate dehydrogenase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0004459
L-lactate dehydrogenase activity
GO:0016491
oxidoreductase activity
GO:0016616
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
GO:0030060
L-malate dehydrogenase (NAD+) activity
Biological Process
GO:0006089
lactate metabolic process
GO:0006090
pyruvate metabolic process
GO:0006099
tricarboxylic acid cycle
GO:0019752
carboxylic acid metabolic process
Cellular Component
GO:0005737
cytoplasm
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2hlp
,
PDBe:2hlp
,
PDBj:2hlp
PDBsum
2hlp
PubMed
10653643
UniProt
Q07841
|MDH_HALMA Malate dehydrogenase (Gene Name=mdh)
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